EP0688840A2 - Composition de revêtement et son utilisation dans la préparation de revêtements multicouches - Google Patents

Composition de revêtement et son utilisation dans la préparation de revêtements multicouches Download PDF

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Publication number
EP0688840A2
EP0688840A2 EP95109313A EP95109313A EP0688840A2 EP 0688840 A2 EP0688840 A2 EP 0688840A2 EP 95109313 A EP95109313 A EP 95109313A EP 95109313 A EP95109313 A EP 95109313A EP 0688840 A2 EP0688840 A2 EP 0688840A2
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EP
European Patent Office
Prior art keywords
mol
acid
component
mole
alpha
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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EP95109313A
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German (de)
English (en)
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EP0688840A3 (fr
Inventor
Klaus Dr. Bederke
Friedrich Herrmann
Hermann Kerber
Thomas Kutzner
Hans Martin Schönrock
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Axalta Coating Systems Germany GmbH and Co KG
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Herberts GmbH
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Publication date
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Publication of EP0688840A2 publication Critical patent/EP0688840A2/fr
Publication of EP0688840A3 publication Critical patent/EP0688840A3/fr
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
    • C08G18/4063—Mixtures of compounds of group C08G18/62 with other macromolecular compounds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04—Polyurethanes

Definitions

  • the invention relates to coating compositions which are particularly suitable for transparent but also pigmented stoving multi-layer coatings, for example in automotive OEM painting, which are distinguished by a high resistance to "acid rain” (acid-rain resistance) and a high scratch resistance.
  • DE-A-39 18 968 describes as scratch-resistant clear lacquers, among other things, coating compositions which harden with free or blocked polyisocyanates and are based on a combination of low molecular weight polyol with a weight average molecular weight of 2000 and a hydroxyl number of 150 to 400 mg KOH / g and hydroxyl-containing acrylic resin a weight average molecular weight of 5,000 to 50,000 and a hydroxyl number of 50 to 180 mg KOH / g.
  • the low molecular weight polyol can be a branched-chain polyester polyol.
  • Cyclohexanedimethanol, trimethylolpropane and succinic anhydride or adipic acid are mentioned as preferred structural components of the branched-chain polyester polyol. Dimer acid should only be used in a small amount if possible. The acid resistance of the paintwork obtained and the scratch resistance are in need of improvement.
  • the object of the invention is to provide coating agents for stoved multi-layer coatings, in particular for automotive series painting, which lead both to coatings with a high acid resistance, in particular an improved resistance to sulfuric acid, and with a high scratch resistance.
  • the hydroxy-functional polyesters used as component A) are polycondensation products from components a1) to a7). Such polyesters are usually made with an excess of alcohol.
  • the OH numbers are preferably 40 to 200, particularly preferably 80 to 180 mg KOH / g, the acid numbers for example 5 to 100, preferably 10 to 40.
  • the weight average molecular weights are, for example, 500 to 6000, preferably 1000 to 4000 g / Mol.
  • Component A) can be produced in various ways from components a1) to a7).
  • the production can be carried out in stages or preferably in a one-pot process.
  • the reactants can be reacted at elevated temperature, e.g. at temperatures of 120 to 240 ° C until the desired degree of polycondensation is reached.
  • Glycidyl esters of alpha, alpha-dialkyl-substituted aliphatic monocarboxylic acids can be used as component a1). Such compounds are commercially available, for example glycidyl esters of alpha, alpha-dialkyl-substituted aliphatic monocarboxylic acids with 9 to 11 carbon atoms, for example of neodecanoic acids, commercial products Cardura R, such as Cardura-E10, from Shell.
  • 2,2-Dialkyl-alkanediols are used as component a2), in particular those with more than 5 carbon atoms in the molecule.
  • polyols with at least one secondary OH group in the molecule can be used. These preferably contain at least two primary OH groups. Examples include glycerin and 1,2,6-hexanetriol.
  • Cyclo aliphatic polycarboxylic acids or their anhydrides are used as component a4).
  • aliphatic dicarboxylic acids are succinic acid, adipic acid, sebacic acid, dodecanedicarboxylic acid.
  • Cycloaliphatic dicarboxylic acids for example 1,2-, 1,3- and 1,4-cyclohexanedicarboxylic acid and 1,2-cyclohexanedicarboxylic anhydride, are particularly preferred.
  • dimer fatty acids and / or dimer diols and / or epsilon-caprolactone are used as component a5).
  • the dimer fatty acids and dimer diols are preferably hydrogenated, i.e. products free from olefinic double bonds.
  • the dimer fatty acids and / or dimer diols are preferably used in amounts of 5 to 15 mol%.
  • Epsilon-caprolactone is preferably used in amounts of 15 to 30 mol%.
  • Hydroxycarboxylic acids are used as component a6). Hydroxycarboxylic acids with a tertiary carboxyl group are particularly preferably used. Preferred examples of this are 2,2-dialkyl-omega-hydroxyalkyl-carboxylic acids-1, the alkyl radicals having, for example, 1 to 6 carbon atoms. Specific examples are 2,2-dimethylolpropionic acid and 3-hydroxypivalic acid.
  • Alpha, beta-unsaturated dicarboxylic acids or their anhydrides can be used as component a7).
  • Examples are maleic acid, fumaric acid, itaconic acid.
  • Maleic anhydride is particularly preferred.
  • Preferred examples of hydroxy-functional polyesters of component A) can be prepared from 2-ethyl-2-butylpropanediol-1,3 as component a2), glycerol and / or hexanetriol-1,2,6 as component a3), 1,2-cyclohexanedicarboxylic acid anhydride and / or 1,4-cyclohexanedicarboxylic acid as component a4), dimer fatty acid, dimer diol and / or epsilon-caprolactone as component a5), dimethylolpropionic acid as component a6) and maleic anhydride as component a7).
  • a particularly preferred polyester component A) is prepared from 2-ethyl-2-butylpropanediol-1,3 as component a2), glycerol as component a3), 1,2-cyclohexanedicarboxylic acid anhydride as component a4), dimer fatty acid as component a5) and dimethylolpropionic acid as component a6).
  • the (meth) acrylic copolymers (component B) contained in the coating composition according to the invention can be prepared, for example, by polymerization using customary processes, e.g. substance, solution or pearl polymerization.
  • customary processes e.g. substance, solution or pearl polymerization.
  • the various polymerization processes are well known and are described, for example, in Houben-Weyl, Methods of Organic Chemistry, 4th Edition, Volume 14/1, pp. 24-255 (1961).
  • the solution polymerization process is preferred for the preparation of the (meth) acrylic copolymers used in the coating composition according to the invention.
  • the solvent is placed in the reaction vessel, heated to boiling temperature and the monomer / initiator mixture is metered in continuously over a certain time.
  • the solution polymerization can also be carried out in such a way that the addition of the monomers takes place at different times, i.e. alternating or in succession.
  • the polymerization is carried out, for example, at temperatures between 60 ° C. and 160 ° C., preferably at 80 ° C. to 140 ° C.
  • the polymerization reaction can be started with known polymerization initiators.
  • Suitable initiators are conventional per and azo compounds which decompose thermally into radicals in a first order reaction.
  • the type and amount of initiator are chosen so that the available radicals are as constant as possible at the polymerization temperature during the feed phase.
  • Examples of preferred initiators for the polymerization are: dialkyl peroxides, such as di-tert-butyl peroxide, di-cumyl peroxide; Diacyl peroxides such as di-benzoyl peroxide, di-lauroyl peroxide; Hydroperoxides, such as cumene hydroperoxide, tert-butyl hydroperoxide; Peresters such as tertiary butyl perbenzoate, tertiary butyl perpivalate, tertiary butyl per 3,5,5-trimethylhexanoate, tertiary butyl per 2-ethylhexanoate; Peroxydicarbonates such as di-2-ethylhexyl peroxydicarbonate, dicyclo-hexyl peroxydicarbonate; Perketals such as 1,1-bis (tert-butylperoxy) -3,5,5-trimethylcyclohexane, 1,1-bis (tert
  • the polymerization initiators in particular the peresters, are preferably used in an amount of 0.2 to 5% by weight of the weight of monomers.
  • Suitable organic solvents which are expediently used in solution polymerization and later also in the coating agent according to the invention, are, for example, glycol ethers, such as ethylene glycol dimethyl ether; Glycol ether esters, such as ethyl glycol acetate, butyl glycol acetate, 3-methoxy-n-butyl acetate, butyl diglycol acetate, methoxypropyl acetate, esters, such as butyl acetate, isobutyl acetate, amyl acetate; Ketones such as methyl ethyl ketone, methyl isobutyl ketone, diisobutyl ketone, cyclohexanone, isophorone; Alcohols such as methanol, ethanol, propanol, butanol; Aromatic hydrocarbons, such as xylene, Solvesso 100 (registered trademark) and aliphatic hydrocarbons can also be used in particular in the blend
  • Conventional chain transfer agents can also be used to regulate the molecular weight, particularly in the preferred solution polymerization.
  • Examples are functionalized or non-functionalized mercaptans, such as mercaptoethanol, n-octyl mercaptan, thioglycolic acid esters, chlorinated hydrocarbons, cumene, dimeric alpha-methylstyrene.
  • the polymerization conditions (reaction temperature, feed time of the monomer mixture, solution concentration) are set up in such a way that the (meth) acrylic copolymers for the coating composition prepared according to the invention preferably have a weight average molecular weight (Mw) (determined by gel permeation chromatography using polystyrene as calibration substance) between 2000 and Have 20000.
  • Mw weight average molecular weight
  • the hydroxyl group-containing (meth) acrylic copolymers of the coating composition prepared according to the invention are preferably in a glass transition temperature range from -20 ° C to + 80 ° C, calculated from the glass transition temperatures of the homopolymers of the individual monomers given in the literature (FOX equation, see for example Polymeric materials, Batzer, 1985, page 307).
  • Alkyl monomers of acrylic acid or methacrylic acid are preferably used as the monomer component for the preparation of the hydroxyl-containing (meth) acrylic copolymers (component B).
  • (Meth) acrylic here means acrylic and / or methacrylic.
  • polyalkylene oxide mono- (meth) acrylates with 2 to 10 alkylene oxide units per molecule can also be used, at least in part.
  • Reaction products from hydroxyalkyl (meth) acrylates with epsilon-caprolactone can also be used.
  • Hydroxy functional monomers such as e.g. Hydroxyalkyl esters of acrylic acid or methacrylic acid are polymerized in such quantities that component B) preferably has an OH number of 30 to 200 mg KOH / g.
  • unsaturated acids can be copolymerized, such as (meth) acrylic acid, maleic acid, fumaric acid and their half esters. They are polymerized in amounts such that an acid number of 1 to 50 mg KOH / g preferably results for component B).
  • Comonomers which differ from the (meth) acrylic monomers can also be used to prepare the copolymers.
  • vinyl monomers such as vinyl aromatics, e.g. Styrene, vinyl toluene, p-methyl styrene and p-tertiary butyl styrene; Vinyl ethers such as isobutyl vinyl ether; Vinyl esters such as vinyl acetate, vinyl propionate, vinyl benzoate, p-tert-butyl vinyl benzoate and vinyl neodecanoate.
  • the comonomers can be used in amounts of up to 50% by weight, for example 10 to 50% by weight, preferably 10 to 30% by weight, in each case based on the weight of the total monomers.
  • Proportionally polyunsaturated monomers can also be used, e.g. Divinylbenzene, ethylene glycol di (meth) acrylate, butanediol di (meth) acrylate. Such monomers are added in small amounts, i.e. in such quantities that the products obtained do not gel.
  • the coating compositions according to the invention contain, as component C), customary lacquer crosslinking agents, for example aminoplast resins and / or blocked and / or non-blocked di- and polyisocyanates customary in paint.
  • customary lacquer crosslinking agents for example aminoplast resins and / or blocked and / or non-blocked di- and polyisocyanates customary in paint.
  • the coating compositions according to the invention preferably contain di- and / or polyisocyanates as crosslinking agents.
  • aminoplast resins are alkylated condensates which are prepared by reacting aminotriazines and amidotriazines with aldehydes.
  • compounds bearing amino or amido groups such as melamine, benzoguanamine, dicyandiamide, urea, N, N'-ethylene urea, in the presence of alcohols, such as methyl, ethyl, propyl, isobutyl, n-butyl, and hexyl alcohol with aldehydes, especially formaldehyde, condensed.
  • reactivity of such amine resins is determined by the degree of condensation, the ratio of the amine or amide component to the formaldehyde and by the type of etherification alcohol used.
  • Melamine resins which are etherified with n- or iso-butanol and whose degree of etherification is ⁇ 1.0 are preferably used.
  • the aminoplast resins can also be present together with polyisocyanates.
  • the proportion of aminoplast resins in the mixture is preferably below 50% by weight, based on the weight of component C).
  • Aliphatic, cycloaliphatic and araliphatic are particularly suitable as polyisocyanates which can be used in a mixture with the aminoplast resins, but preferably also alone as crosslinking component C).
  • Hexamethylene-1,6-diisocyanate, 3,5,5-trimethylhexamethylene-1,6-diisocyanate, isophorone diisocyanate, 1,3-bis (isocyanatomethyl) cyclohexane, bis-isocyanato-cyclohexylmethane, tetramethylxylylene diisocyanate (TMXDI) are preferably used as diisocyanates.
  • polyisocyanates for example, polyisocyanates containing biuret groups, for example reaction products of 3 moles of hexamethylene diisocyanate with 1 mole of water with an NCO content of approximately 22%, or polyisocyanates containing isocyanurate groups, which are prepared, for example, by trimerizing 3 moles of hexamethylene diisocyanate are with an NCO content of about 21.5%, or polyisocyanates containing urethane groups, which are, for example, reaction products of 3 moles of aliphatic or cycloaliphatic diisocyanates with 1 mole of triol, for example trimethylolpropane.
  • Isophorone diisocyanate is the preferred aliphatic diisocyanate.
  • the polyisocyanate crosslinking agents can be partial or, if a longer shelf life, i.e. a one-component coating agent is desired, be completely blocked with active hydrogen-containing monofunctional compounds.
  • the choice of the blocking agent which can be removed again thermally with the reformation of the free isocyanate groups depends on the prevailing stoving conditions during the curing of the coating agent according to the invention.
  • the polyisocyanate crosslinking agents are preferably used uncapped.
  • customary blocking agents for example CH-acidic, NH- or OH-functional compounds
  • blocking agents can be used as blocking agents, which enable crosslinking with hydroxyl-functional binders under curing conditions.
  • blocking agents that can be used are oximes and CH-acidic compounds such as malone or acetoacetic esters. It may be advantageous to use different capping agents at the same time, which can take place within a polyisocyanate molecule or in a mixture.
  • the coating compositions according to the invention may additionally contain customary auxiliaries, for example: leveling agents, for example based on (meth) acrylic homopolymers, silicone oils, plasticizers such as phosphoric, phthalic or citric esters, matting agents, such as pyrogenic silicon oxide.
  • leveling agents for example based on (meth) acrylic homopolymers, silicone oils, plasticizers such as phosphoric, phthalic or citric esters, matting agents, such as pyrogenic silicon oxide.
  • Curing accelerators for example phosphoric acid, phosphoric acid esters, dicarboxylic acid half esters, citric acid; organic metal salts, such as Dibutyltin dilaurate, zinc naphthenate, and also compounds containing tertiary amino groups, such as triethylamine.
  • the coating compositions according to the invention can be formulated in aqueous and non-aqueous form.
  • aqueous coating compositions it is advantageous to use components A) and B) which have an acid number range above about 30. These components containing acid functions can then be partially or completely neutralized with amines and then converted into the aqueous phase by dilution with water.
  • the coating compositions according to the invention are particularly suitable for producing a transparent cover layer (clear lacquer layer) in the production of oven-drying multilayer coatings.
  • the top layer can be applied, for example, by the wet-on-wet method, whereupon both layers are hardened together.
  • the invention therefore also relates to the process for the production of multilayer coatings or the use of the coating compositions for their production.
  • the solvent-based coating compositions according to the invention can be applied as transparent topcoats to layers of aqueous or solvent-based base sheets for curable multi-layer coatings.
  • Pigmented coating agents can also be provided.
  • Conventional organic and / or inorganic color pigments and / or fillers such as titanium dioxide, micronized titanium dioxide, iron oxide pigments, carbon black, silicon dioxide, barium sulfate, micronized mica, talc, azo pigments, phthalocyanine pigments, quinacridone or pyrrolopyrrole pigments can be used for this purpose.
  • the coating compositions according to the invention are applied by known processes, such as spraying, dipping, rolling or knife coating.
  • the top coat is applied to the substrate, which may already have been provided with further layers of lacquer.
  • the coating compositions according to the invention can also be applied using supercritical carbon dioxide as a solvent in the spraying process.
  • the salary of organic solvents can be greatly reduced.
  • the applied coating agent is preferably crosslinked by heating.
  • the stoving temperatures are preferably between 80 and 160 ° C., particularly preferably between 120 to 150 ° C.
  • the curing times are, for example, in the order of 20 to 40 minutes.
  • the crosslinking can also be carried out at lower temperatures, for example at 20 to 80 ° C.
  • the layer thickness of the baked film is approx.
  • a preferred embodiment is the application of the coating composition according to the invention as a clear lacquer coating on a basecoat. You can work wet-on-wet, or the basecoat is previously dried by heating. The two layers have particularly good adhesion.
  • basecoats can be overcoated, which may contain customary topcoat pigments; Metallic pigments.
  • Polyester, polyurethane or acrylate resins are preferably used as the binder base of the basecoat.
  • These binders can optionally be crosslinked, e.g. Melamine or isocyanate derivatives are crosslinked.
  • the coating compositions according to the invention are particularly suitable for topcoats or clearcoats, which are preferably used in the motor vehicle sector, but also in other areas.
  • the use of the coating agent according to the invention in multi-layer coating is particularly suitable for automotive series painting, but it can also be used for other purposes, such as in car refinishing, for household appliances or in the furniture industry.
  • the coating compositions according to the invention are particularly suitable for producing a transparent cover layer of an oven-drying multilayer coating. They are particularly suitable for the serial painting of motor vehicle bodies and their parts.
  • topcoat layers produced using the coating compositions according to the invention e.g. Clear varnish layers are characterized by superior acid resistance, especially sulfuric acid resistance and excellent scratch resistance.
  • the polyester resin solution has a solids content of 70.2% and a viscosity of 1330 mPa.s / 25 ° C.
  • the polyester resin solution has a solids content of 70.6% and a viscosity of 1200 mPa.s / 25 ° C.
  • the polyester resin solution has a solids content of 70.9% and a viscosity of 2200 mPa.s / 25 ° C.
  • the polyester resin solution has a solids content of 70.9% and a viscosity of 1200 mPa.s / 25 ° C.
  • the polyester resin solution has a solids content of 69.7% and a viscosity of 555 mPa.s / 25 ° C.
  • the mixture is then post-polymerized for 4 hours at 143 ° C., cooled to 80 ° C. and diluted with 50 g Solvesso 100 and 20 g n-butanol.
  • the polymer solution has a solids content of 65.1% and a viscosity of 2460 mPa.s / 25 ° C.
  • Example 8 The procedure is analogous to Example 8, with the difference that 196 parts of the polyester resin solution from Example 1 and 488 parts of the (meth) acrylic copolymer solution from Example 7 were used. In 100 parts of this solution, 35 parts of a 69.3% solution of a mixture of customary lacquer hexamethylene diisocyanate and isophorone diisocyanate trimer in a ratio of 1: 1, dissolved in xylene, Solvesso 100, butyl acetate and methoxypropyl acetate in a ratio of 25:20:30:30 homogeneously stirred.
  • the stroke-push method with the Erichsen-Peters block, type no. 265 was used to test the clear lacquers for scratch resistance.
  • the weight is 2 kg.
  • a 2.5 mm thick wool felt, dimensions 30 x 50 mm, is glued under the sanding block with Velcro.
  • 1 g of a water-soluble abrasive paste is evenly distributed on the contact surface. It will 10 double strokes in 9 s.
  • the stroke thrust is parallel to the 75 mm edge of the block, the grinding path is 90 mm in one direction. It is then rinsed with cold water, dried and a gloss measurement is carried out at an angle of 20 °.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Paints Or Removers (AREA)
EP95109313A 1994-06-20 1995-06-16 Composition de revêtement et son utilisation dans la préparation de revêtements multicouches Withdrawn EP0688840A3 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE4421525 1994-06-20
DE4421525 1994-06-20

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EP0688840A2 true EP0688840A2 (fr) 1995-12-27
EP0688840A3 EP0688840A3 (fr) 1996-08-07

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WO1996034924A1 (fr) * 1995-05-02 1996-11-07 E.I. Du Pont De Nemours And Company Composition de revetement resistant au rayage
WO1998003598A1 (fr) * 1996-07-24 1998-01-29 Basf Coatings Ag Agent de revetement a base de resine polyacrylate ramifiee contenant des groupes hydroxyle, modifiee par polyester, et son utilisation pour realiser une mise en peinture multicouche
EP0882750A3 (fr) * 1997-06-05 1999-02-24 Rohm And Haas Company Composition de revêtement thermodurcissableà faible teneur en composés volatiles organiques et à teneur élevée en matières solides et procédé pour son procédé
US5932675A (en) * 1989-06-05 1999-08-03 Commonwealth Scientific And Industrial Research Organisation Free-radical chain transfer polymerization process
US5977256A (en) * 1996-04-29 1999-11-02 E.I. Du Pont De Nemours And Company Scratch-resistant coating composition
WO2000066670A1 (fr) * 1999-04-30 2000-11-09 The Valspar Corporation Composition de revetement reticulable
US6461688B1 (en) 1999-04-29 2002-10-08 The Valspar Corporation Coating composition for metal substrates
WO2007020269A1 (fr) * 2005-08-17 2007-02-22 Akzo Nobel Coatings International B.V. Composition de revetement comprenant un polyacrylate polyol, un polyester polyol, et un agent de reticulation a fonctions isocyanates
WO2007120431A1 (fr) * 2006-03-29 2007-10-25 Ppg Industries Ohio, Inc. Formules pour revêtement transparent de résistance à la rayure améliorée
WO2010112441A1 (fr) 2009-03-31 2010-10-07 Akzo Nobel Coatings International B.V. Durcissement de revêtements par rayonnement
US8143341B2 (en) 2006-03-29 2012-03-27 Ppg Industries Ohio, Inc Aqueous coating compositions
WO2013113642A1 (fr) 2012-01-30 2013-08-08 Akzo Nobel Coatings International B.V. Procédé de réparation et composition d'apprêt
WO2013117972A1 (fr) * 2012-02-10 2013-08-15 Basf Japan Ltd. Composition de peinture claire de type à un seul liquide et procédé de formation de film de peinture multicouche dans lequel elle est utilisée
WO2013131835A2 (fr) 2012-03-07 2013-09-12 Akzo Nobel Coatings International B.V. Composition de revêtement liquide non aqueux
WO2014192314A1 (fr) 2013-05-31 2014-12-04 凸版印刷株式会社 Support de stratification pour le transfert et imprimé
EP2910612A1 (fr) * 2014-02-20 2015-08-26 BASF Coatings GmbH Compositions de produits de revêtement, revêtements ainsi fabriqués et leur utilisation
US9745401B2 (en) 2008-10-22 2017-08-29 Akzo Nobel Coatings International B.V. Coating composition comprising a polyisocyanate and a polyol
WO2017199982A1 (fr) 2016-05-16 2017-11-23 凸版印刷株式会社 Support d'informations optique et son procédé de fabrication
US10471758B2 (en) 2015-02-03 2019-11-12 Toppan Printing Co., Ltd. Optical information medium

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AT408659B (de) * 1999-12-23 2002-02-25 Solutia Austria Gmbh Wässriges überzugsmittel
CA2399582A1 (fr) * 2000-02-08 2001-08-16 The C.P. Hall Company Compositions a base de resine de polyol de polyester non lineaire a faible teneur en compose organique volatil
DE10317645A1 (de) * 2003-04-17 2004-11-04 Cognis Deutschland Gmbh & Co. Kg Dimerdiol(meth)acrylate als Mattierungsmittel
WO2005054386A1 (fr) * 2003-12-08 2005-06-16 Natoco Co., Ltd. Composition de revetement et article revetu au moyen de celle-ci
DE602006013835D1 (de) * 2005-08-17 2010-06-02 Akzo Nobel Coatings Int Bv Beschichtungszusammensetzung, enthaltend ein polyisocyanat und ein polyol
EP2079532A1 (fr) * 2006-10-25 2009-07-22 Brian Alzano Mayes Club de golf
US20170101502A1 (en) * 2015-10-13 2017-04-13 Eastman Chemical Company Systems and methods for forming polyurethanes
CN113150257B (zh) * 2021-02-26 2023-06-13 南雄市三本化学科技有限公司 一种聚酯树脂及其制备方法和在湿碰湿工艺中的应用
WO2023167677A1 (fr) * 2022-03-03 2023-09-07 Inx International Ink Co. Compositions de réticulation liquides stables pour encres durcissables à la chaleur

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WO2014192314A1 (fr) 2013-05-31 2014-12-04 凸版印刷株式会社 Support de stratification pour le transfert et imprimé
US10059086B2 (en) 2013-05-31 2018-08-28 Toppan Printing Co., Ltd. Laminated transfer medium and printed matter
EP2910612A1 (fr) * 2014-02-20 2015-08-26 BASF Coatings GmbH Compositions de produits de revêtement, revêtements ainsi fabriqués et leur utilisation
WO2015124231A1 (fr) * 2014-02-20 2015-08-27 Basf Coatings Gmbh Compositions d'agent de revêtement et revêtements produits à partir de telles compositions ainsi que leur utilisation
US10005923B2 (en) 2014-02-20 2018-06-26 Basf Coatings Gmbh Coating material compositions and coatings produced therefrom, and use thereof
US10471758B2 (en) 2015-02-03 2019-11-12 Toppan Printing Co., Ltd. Optical information medium
WO2017199982A1 (fr) 2016-05-16 2017-11-23 凸版印刷株式会社 Support d'informations optique et son procédé de fabrication

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